EP2473472A2 - Process for the synthesis of fluorinated ethers of aromatic acids - Google Patents

Process for the synthesis of fluorinated ethers of aromatic acids

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Publication number
EP2473472A2
EP2473472A2 EP10814464A EP10814464A EP2473472A2 EP 2473472 A2 EP2473472 A2 EP 2473472A2 EP 10814464 A EP10814464 A EP 10814464A EP 10814464 A EP10814464 A EP 10814464A EP 2473472 A2 EP2473472 A2 EP 2473472A2
Authority
EP
European Patent Office
Prior art keywords
integer
functionality
ich
group
cch
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP10814464A
Other languages
German (de)
English (en)
French (fr)
Inventor
Joachim C. Ritter
Kenneth Gene Moloy
Neville Everton Drysdale
Joel M. Pollino
Surbhi Mahajan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of EP2473472A2 publication Critical patent/EP2473472A2/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/80—Phthalic acid esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
    • C07C65/24—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups polycyclic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/80—Phthalic acid esters
    • C07C69/82—Terephthalic acid esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/84—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring
    • C07C69/92—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of monocyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of a six-membered aromatic ring with etherified hydroxyl groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/682—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens

Definitions

  • This invention relates to the manufacture of fluorinated ethers of aromatic acids or hydroxy aromatic acids, which are valuable for a variety of purposes such as use as surfactants, intermediates or as monomers to make polymers .
  • Fluorinated organic compounds have been used in a wide variety of applications, for example, in surface treatments, as intermediates in the synthesis of compounds such as pharmaceuticals, and as monomers in the synthesis of polymers with highly valued properties .
  • the fluorinated compounds are applied as a topical treatment, but their effectiveness decreases over time because of material loss resulting from wear and washing.
  • Ar is a C6 ⁇ C2o monocyclic or polycyclic aromatic nucleus
  • n and m are each independently a nonzero value
  • n+m is less than or equal to 8
  • Rf is a fluorinated alkyl, alkaryl, aralkyl, or aryl group, optionally containing one or more ether linkages -0- and
  • R is H or a branched or linear Ci t0 10 alkyl group.
  • Another embodiment of this invention provides a process for preparing a compound, monomer, oligomer or polymer by preparing a fluorinated ether of an aromatic acid as is represented by the structure of Formula I, and then subjecting the ether so produced to a reaction
  • Ar is a C6 ⁇ C2o monocyclic or polycyclic aromatic nucleus , n and m are each independently a nonzero value, n+m is less than or equal to 8 ,
  • Rf is a fluorinated alkyl, alkaryl, aralkyl, or aryl group, optionally containing one or more ether linkages - 0- ;
  • R is H or a branched or linear Ci t o 10 alkyl group.
  • Formula I include without limitation:
  • alkyl denotes a univalent group derived from an alkane by removing a hydrogen atom from any carbon atom: -C x H 2x+ i where x ⁇ 1.
  • aryl denotes a univalent group whose free valence is to a carbon atom of an aromatic ring.
  • aralkyl denotes an alkyl group which bears an aryl group.
  • benzyl group i.e. the radical
  • alkaryl denotes an aryl group which bears an alkyl group.
  • alkyl group Some examples are the 4-methylphenyl radical,
  • the mesityl group i.e. 2 , 4 , 6-trimethylphenyl
  • the 2 , 6-diisopropylphenyl group i.e., the (CH 3 CHCH 3 ) 2C6H3- radical
  • Ar is an n+m valent C6 ⁇ C2o monocyclic or polycyclic aromatic nucleus formed by the removal of n+m hydrogens from different carbon atoms on the aromatic ring, or on the aromatic rings when the structure is polycyclic.
  • the radical "Ar” may be substituted or unsubstituted; when unsubstituted, it contains only carbon and hydrogen.
  • a suitable Ar group is
  • compositions of Formula I can be made by the following copper-catalyzed process: (a) contacting a halogenated aromatic acid that is described by the structure of Formula IV
  • each X is independently CI, Br, or I, and Ar, n and m are as set forth above, with
  • ligand that coordinates to copper, wherein said ligand is a diamine, diketones, Schiff Base, or amino acid,
  • step (b) heating the reaction mixture to form the m- basic salt of the product of step (a) , as described by the structure of Formula V;
  • m-basic salt is the salt formed from an acid that contains in each molecule m acid groups having a replaceable hydrogen atom.
  • R f groups that are not attached to the ether oxygen in Formula I via a CF 2 group or a
  • CF 2 CH 2 CH2 group include without limitation:
  • 2- bromobenzoic acid is available from Aldrich Chemical Company (Milwaukee, Wisconsin) . It can be synthesized, however, by oxidation of bromomethylbenzene as described in Sasson et al, Journal of Organic Chemistry (1986) , 51(15), 2880-2883.
  • halogenated aromatic acids that can be used include without limitation 2,5- dibromobenzoic acid, 2-bromo-5-nitrobenzoic acid, 2- bromo-5-methylbenzoic acid, 2-chlorobenzoic acid, 2,5- dichlorobenzoic acid, 2-chloro-3,5-dinitrobenzoic acid, 2-chloro-5-methylbenzoic acid, 2-bromo-5-methoxybenzoic acid, 5-bromo-2-chlorobenzoic acid, 2 , 3-dichlorobenzoic acid, 2-chloro-4-nitrobenzoic acid, 2,5- dichloroterephthalic acid, 2-chloro-5-nitrobenzoic acid, 2 ,5-dibromoterephthalic acid, and 2,5- dichloroterephthalic acid, all of which are commercially available.
  • the halogenated aromatic acid is 2 ,5-dibromoterephthalic acid or 2 , 5-dichloroterephthalic acid.
  • the copper source is a Cu(I) salt, a Cu(II) salt, or mixtures thereof. Examples include without limitation CuCl, CuBr, Cul, Cu 2 S0 4 , CuN0 3 , CuCl 2 , CuBr 2 , Cul 2 , CuS0 4 , and Cu(N0 3 ) 2 .
  • the selection of the copper source may be made in relation to the identity of the halogenated aromatic acid used.
  • the starting halogenated aromatic acid is a bromobenzoic acid
  • CuCl, CuBr, Cul, Cu 2 S0 , CuN0 3 , CuCl 2 , CuBr 2 , Cul 2 , CuS0 4 , and Cu( 0 3 ) 2 will be included among the useful choices.
  • the starting halogenated aromatic acid is a chlorobenzoic acid
  • CuBr, Cul, CuBr 2 and Cul 2 will be included among the useful choices .
  • compositions described by Formula I wherein (1) R is not H, or (2) R is H and R f is attached to the ether oxygen in Formula I via a CF2 group or a CF2CH2CH2 group can be made using synthetic routes other than the copper- catalyzed processes described above.
  • compositions can be prepared, for example, by the addition of a phenol to a fluorinated olefin.
  • compositions can be made by the coupling of alcohols and phenols to form aryl ethers using triphenylphosphine and diethyl azodicarboxylate (“DEAD”) .
  • DEAD diethyl azodicarboxylate
  • compositions or compounds of the above Formula I can be applied, for example, to fibers, yarns, carpets, garments, films, molded parts, paper and
  • compositions or compounds of Formula I as prepared herein can thus be used in turn in the synthesis of products such as a compound, a monomer, or an oligomer or polymer thereof.
  • These produced materials may have one or more of ester functionality, ether functionality, amide functionality, imide functionality, imidazole functionality, thiazole functionality, oxazole
  • a Formula I compound may, as desired, be isolated and recovered as described above. It may also be subjected with or without recovery from the reaction mixture to further steps to convert it to another product such as another compound (e.g. a monomer), or an oligomer or a polymer. Another embodiment of a process hereof thus provides a process for converting a Formula I compound, through one or more reactions, into another compound, or into an oligomer or a polymer.
  • a Formula I compound may be made by a process such as described above, and then may be subjected, for example, to a polymerization reaction to prepare an oligomer or polymer therefrom, such as those having ester functionality or amide functionality, or a pyridobisimidazole-2 , 6- diyl (2 , 5-dihydroxy-p-phenylene) polymer .
  • the compounds of Formula I made by the process disclosed herein, in particular the dimethyl esters, can be used in condensation polymerizations to produce fluorinated condensation polymers, e.g. those including without limitation polyesters, polyamides, polyimides, and polybenzimidazoles .
  • Representative reactions involving a material of this invention, or a derivative of such material, such as a diester include, for example, making a polyester from one or more compounds of Formula I and either diethylene glycol or triethylene glycol in the presence of 0.1% of Zn3 (1303)2 in 1- methylnaphthalene under nitrogen, according to the method taught in US 3,047,536 (which is incorporated in its entirety as a part hereof for all purposes) .
  • a fluorinated ether of aromatic acid is suitable for copolymerization with a dibasic acid and a glycol to prepare a heat-stabilized fluorinated polyester according to the method taught in US 3,227,680 (which is
  • diols useful to make a polyester from a Formula I compound are those that are derived from a fermentation process, and another embodiment of this invention thus involves a process for making from a
  • Formula I compound an oligomer or polymer that further includes a step of providing a diol to such a process from a fermentation process.
  • a Formula I compound may be converted into a polyamide oligomer or polymer by reaction with a diamine in a process in which, for example, the polymerization takes place in solution in an organic compound that is liquid under the conditions of the reaction, is a solvent for both the Formula I compound and the diamine, and has a swelling or partial salvation action on the polymeric product.
  • the reaction may be effected at moderate temperatures, e.g. under 100°C, and is preferably effected in the presence of an acid acceptor that is also soluble in the chosen solvent.
  • Suitable solvents include methyl ethyl ketone, acetonitrile, N,N-dimethylacetamide dimethyl formamide containing 5% lithium chloride, and N- methyl pyrrolidone containing a quaternary ammonium chloride such as methyl tri-n-butyl ammonium chloride or methyl-tri-n-propyl ammonium chloride.
  • a quaternary ammonium chloride such as methyl tri-n-butyl ammonium chloride or methyl-tri-n-propyl ammonium chloride.
  • a Formula I compound may also be converted into a polyamide oligomer or polymer by reaction with a diamine in a process in which, for example, a solution of the diamine in a solvent may be contacted in the presence of an acid acceptor with a solution of the Formula I compound in a second solvent that is immiscible with the first to effect polymerization at the interface of the two phases.
  • the diamine may, for example, be dissolved or dispersed in a water containing base with the base being used in sufficient quantities to neutralize the acid generated during polymerization.
  • Sodium hydroxide may be used as the acid acceptor.
  • Preferred solvents for the diacid(halide) are tetrachloroethylene ,
  • the solvent for the Formula I compound should be a relative non- solvent for the amide reaction product, and be relatively immiscible in the amine solvent.
  • a preferred threshold of immiscibility is as follows : an organic solvent should be soluble in the amine solvent not more than between 0.01 weight percent and 1.0 weight percent.
  • the solution of acid chloride is added to the aqueous slurry. Contacting is generally carried out at from 0°C to 60 °C, for example, for from about 1 second to 10 minutes, and preferably from 5 seconds to 5 minutes at room temperature. Polymerization occurs rapidly.
  • a fluorinated ether of aromatic acid can also be polymerized with the trihydrochloride-monohydrate of tetraaminopyridine in a condensation polymerization in strong polyphosphoric acid under slow heating above 100°C up to about 180°C under reduced pressure, followed by precipitation in water, as disclosed in US 5,674,969 (which is incorporated in its entirety as a part hereof for all purposes) ; or by mixing the monomers at a temperature from about 50 °C to about 110 °C, and then 145°C to form an oligomer, and then reacting the oligomer at a temperature of about 160 °C to about 250 °C as
  • the polymer that may be so produced may be a pyridobisimidazole-2 , 6-diyl (2 , 5-dialkoxy-p- phenylene) polymer or a pyridobisimidazole-2 , 6-diyl (2 ,5- diareneoxy-p-phenylene) polymer such as a poly (1,4- (2,5- diareneoxy) phenylene-2 , 6-pyrido [2 , 3-d: 5,6- d' ]bisimidazole) polymer.
  • the pyridobisimidazole portion thereof may, however, be replaced by any one or more of a benzobisimidazole, benzobisthiazole, benzobisoxazole, pyridobisthiazole and a pyridobisoxazole ; and the 2,5- dialkoxy-p-phenylene portion thereof may be replaced by an alkyl or aryl ether of one or more of isophthalic acid, terephthalic acid, 2,5-pyridine dicarboxylic acid, 2 , 6-naphthalene dicarboxylic acid, 4 , 4' -diphenyl
  • the polymer prepared in such manner may, for example , contain one or more of the following units :
  • pyridobisimidazole-2 6-diyl (2 , 5-dialkoxy-p- phenylene) and/or pyridobisimidazole-2 , 6-diyl (2 ,5- diphenoxy-p-phenylene) units ; units selected from the group consisting of pyridobisimidazole-2,6-diyl(2,5-dimethoxy-p-pheny1ene) , pyridobisimidazole-2,6-diyl(2,5-diethoxy-p-pheny1ene) , pyridobisimidazole-2 , 6-diyl (2 ,5-dipropoxy-p-phenylene) , pyridobisimidazole-2, 6-diyl (2, 5-dibutoxy-p-phenylene) and pyridobisimidazo1e-2 , 6-diy1 (2 , 5-diphenoxy-p-pheny1ene
  • the reaction was cooled to -5°C, followed by the addition of triphenylphosphine (1.5 g, 0.0057 mol, 1.2 eq) , ⁇ , ⁇ , 2#,2ff-perfluorooctanol (2.1 g, 0.0057 mol, 1.2 eq) , then by the dropwise addition of a solution of diethyl azodicarboxylate (DEAD) (1.0 g, 0.0057 mol, 1.2 eq) in 5 mL of dry tetrahydrofuran. The DEAD addition was slightly exothermic (-5°C to 5°C) . The cold bath was removed and the reaction was stirred overnight at ambient temperature .
  • DEAD diethyl azodicarboxylate
  • each of the formulae shown herein describes each and all of the separate, individual compounds that can be formed in that formula by (1) selection from within the prescribed range for one of the variable radicals, substituents or numerical coefficients while all of the other variable radicals, substituents or numerical coefficients are held constant, and (2) performing in turn the same selection from within the prescribed range for each of the other variable radicals, substituents or numerical coefficients with the others being held constant.
  • a plurality of compounds may be described by selecting more than one but less than all of the members of the whole group of radicals, substituents or numerical
  • variable radicals, substituents or numerical coefficients When the selection made within the prescribed range for any of the variable radicals, substituents or numerical coefficients is a subgroup containing (i) only one of the members of the whole group described by the range, or (ii) more than one but less than all of the members of the whole group, the selected member (s) are selected by omitting those member (s) of the whole group that are not selected to form the subgroup.
  • the compound, or plurality of compounds may in such event be characterized by a definition of one or more of the variable radicals, substituents or numerical
  • range includes the endpoints thereof and all the individual integers and fractions within the range, and also includes each of the narrower ranges therein formed by all the various possible combinations of those endpoints and internal integers and fractions to form subgroups of the larger group of values within the stated range to the same extent as if each of those narrower ranges was explicitly recited.
  • range of numerical values is stated herein as being greater than a stated value, the range is nevertheless finite and is bounded on its upper end by a value that is operable within the context of the invention as described herein.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Artificial Filaments (AREA)
EP10814464A 2009-09-02 2010-09-02 Process for the synthesis of fluorinated ethers of aromatic acids Withdrawn EP2473472A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US23910709P 2009-09-02 2009-09-02
PCT/US2010/047595 WO2011028851A2 (en) 2009-09-02 2010-09-02 Process for the synthesis of fluorinated ethers of aromatic acids

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EP2473472A2 true EP2473472A2 (en) 2012-07-11

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EP10814464A Withdrawn EP2473472A2 (en) 2009-09-02 2010-09-02 Process for the synthesis of fluorinated ethers of aromatic acids

Country Status (8)

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US (1) US8779186B2 (https=)
EP (1) EP2473472A2 (https=)
JP (1) JP2013503886A (https=)
KR (1) KR20120057642A (https=)
CN (1) CN102596885A (https=)
IN (1) IN2012DN02013A (https=)
TW (1) TW201127809A (https=)
WO (1) WO2011028851A2 (https=)

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Publication number Priority date Publication date Assignee Title
US8513454B2 (en) * 2011-12-08 2013-08-20 E I Du Pont De Nemours And Company Preparation of (phosphonyl) aromatic diesters and acids
US11492318B2 (en) 2017-05-19 2022-11-08 Etna-Tec, Ltd. Methods for making functionalized fluorinated monomers, fluorinated monomers, and compositions for making the same

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US3227680A (en) * 1961-03-07 1966-01-04 Eastman Kodak Co Heat stabilization of polyesters with built-in stabilizers
GB1135462A (en) * 1966-05-13 1968-12-04 Ici Ltd Aromatic polyamides
CA1132397A (en) * 1979-02-28 1982-09-28 Hendrik E. Kokelenberg Fluorine-containing surfactants and their use in hydrophilic colloid coating compositions and light-sensitive silver halide materials
US4737571A (en) 1986-01-17 1988-04-12 E. I. Du Pont De Nemours And Company Preparation of aromatic polyamide with solvent system comprising N-alkyl substituted amide and quaternary ammonium compound
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JP2010513504A (ja) * 2006-12-21 2010-04-30 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 芳香族酸のエーテルの合成方法

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Publication number Publication date
KR20120057642A (ko) 2012-06-05
CN102596885A (zh) 2012-07-18
US8779186B2 (en) 2014-07-15
WO2011028851A3 (en) 2011-05-19
US20110060116A1 (en) 2011-03-10
TW201127809A (en) 2011-08-16
JP2013503886A (ja) 2013-02-04
WO2011028851A2 (en) 2011-03-10
IN2012DN02013A (https=) 2015-07-24

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